-
Genomic profiling of esthesioneuroblastoma
Study
EGAS00001003225
-
Genomic landscape of oral cancers (Illumina RNA-Seq)
Study
EGAS00001003237
-
Genetic alterations in metastatic uveal melanoma
Study
EGAS00001003303
-
Inherited genetic predisposition to childhood acute lymphoblastic leukemia investigated using a genome wide association study.
Study
EGAS00001002809
-
Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers.
Study
EGAS00001002479
-
Cryptic Relatedness in the Singapore Living Biobank Project
Study
EGAS00001002619
-
Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma
Study
EGAS00001002492
-
Genetic and expression landscape of Waldenstrom macroglobulinemia
Study
EGAS00001003603
-
Phylogenetic evolution of metastatic melanoma.
Study
EGAS00001003582
-
Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Study
EGAS00001002182
-
Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811
-
Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723
-
Physiological and genetic adaptations to diving in Sea Nomads
Study
EGAS00001002823
-
Cistrome-partitioning reveals convergence of somatic mutations and risk-variants on master transcription regulators in primary prostate tumors
Study
EGAS00001003928
-
Whole-exome sequencing of the transposition of the great arteries
Study
EGAS00001004175
-
Exome-sequencing of two UFM individuals and their Fragile X family members.
Study
EGAS00001001737
-
InsPIRE islets
Study
EGAS00001003997
-
Whole Exome Sequencing of Spanish Patients diagnosed with rare ophtalmogenetic disorders: Macular Dystrophy, Retinitis Pigmentosa and Leber's congenital amaurosis.
Study
EGAS00001004084
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia (CML)
Study
EGAS00001001751
-
Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
-
High-resolution analyses of human sperm dynamic methylome reveals thousands of novel age-related epigenetic alterations
Study
EGAS00001004168
-
Sex-biased patterns shaped the genetic history of Roma
Study
EGAS00001004207
-
Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer
Study
EGAS00001005549
-
Ashkenazi Jewish Leukoencephalopathy
Study
EGAS00001001767
-
Characterization of a human iPSC-derived endocrine pancreas model
Study
EGAS00001001803
-
Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens
Study
EGAS00001004459
-
Fine-Scale Genomic Analyses Of Admixed Individuals Reveal Unrecognized Genetic Ancestry Components In Argentina
Study
EGAS00001004492
-
Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma
Study
EGAS00001004546
-
SNP array files, IDAT files, from 34 members of a Family with a high prevalence of psychosis
Study
EGAS00001004592
-
Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
-
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
-
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
-
Whole exome sequencing of Finnish hereditary breast cancer families
Study
EGAS00001001835
-
Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Study
EGAS00001001838
-
The dataset of Southeast Borneo individuals (Banjar and Ngaju ethnic groups) was used as comparative data to determine the Asian parental population of the Malagasy. Our study found strong support for an origin of the Asian ancestry of Malagasy among the Banjar.
Study
EGAS00001001841
-
Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
-
Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree
Study
EGAS00001001862
-
Summary statistics of meta-analysis using two genome-wide association study of inflammatory bowel disease in Koreans.
Study
EGAS00001005026
-
A rare CTSC mutation in Papillon-Lefèvre Syndrome
Study
EGAS00001005040
-
Recent genetic history of Denmark
Study
EGAS00001001868
-
Exome and RNA sequencing of relapsed TCF3-PBX1 t(1;19) acute lymphoblastic leukemia
Study
EGAS00001001876
-
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Study
EGAS00001005187
-
Variation in the Glucose Transporter gene SLC2A2 is associated with glycaemic response to metformin
Study
EGAS00001001875
-
Investigating genetic susceptibility to rheumatic heart disease in Oceania
Study
EGAS00001001881
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889
-
The genetic scenario of Mercheros: an under-represented population within the Iberian Peninsula
Study
EGAS00001005360
-
X chromosomal genetic variants are associated with childhood obesity
Study
EGAS00001002738
-
Integrated genetic and epigenetic analysis of myxofibrosarcoma
Study
EGAS00001002889
-
Geographical structure and differential natural selection among North European populations
Study
EGAS00000000033
-
Carbamazepine-induced hypersensitivity reactions in Europeans
Study
EGAS00000000037
-
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
Study
EGAS00000000097
-
Identification of genetic etiology of CAMRQ2
Study
EGAS00000000099
-
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
Study
EGAS00000000129
-
DAC_for_study___Screening_for_human_epigenetic_variation_at_CpG_islands
Dac
EGAC00001000043
-
Genetic_variation_in_Kuusamo
Study
EGAS00001000020
-
An exome sequencing pilot study of HIV elite-long term non progressors and rapid progressors
Study
EGAS00001000057
-
Contribution of allelic imbalance to colorectal cancer
Study
EGAS00001002966
-
Determination of the molecular nature of the Vel blood group by exome sequencing
Study
EGAS00001000069
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
Functional_characterisation_of_CpG_islands_in_human_and_mouse_tissues
Study
EGAS00001000075
-
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Study
EGAS00001000076
-
Novel regional age-associated DNA methylation changes within human common disease-associated loci
Study
EGAS00001001910
-
Dilgom_Exome
Study
EGAS00001000086
-
Unraveling_the_genetic_basis_of_a_collagen_migration_defect_in_patients_with_a_combined__platelet_dysfunction_and_reduced_bone_density
Study
EGAS00001000093
-
Exome sequencing
Study
EGAS00001005761
-
Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Study
EGAS00001000133
-
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
-
ENGAGE___Amendment__500_genes_exon_sequencing_
Study
EGAS00001000137
-
Genetic_background_for_the_major_psychiatric_disorders_in_the_general_Finnish_population
Study
EGAS00001000162
-
Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population
Study
EGAS00001000229
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299
-
Identifying genetic consequences of Epstein-Barr Virus transformation by comparing an individual’s genomic DNA with that of its lymphoblastoid cell line.
Study
EGAS00001000323
-
Identification of the dismal subtype of B-ALL with dysregulation of CDX2 and UBTF
Study
EGAS00001005863
-
Understanding_population_genetics_and_patterns_of_genome_wide_heterozygosity_in_a_sample_of_the_Croatian_isolated_populations__ESGIDalmatians_
Study
EGAS00001000336
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
-
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
Study
EGAS00001000399
-
Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A
Study
EGAS00001000568
-
Cell-type, allelic and genetic signatures in the human pancreatic beta cell transcriptome
Study
EGAS00001000442
-
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
-
Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques.
Study
EGAS00001000506
-
Chromosome Y Philogeny in Sardinia
Study
EGAS00001000532
-
Detection of Clinically Relevant Genetic Variantsin Autism Spectrum Disorderby Whole-Genome Sequencing
Study
EGAS00001000850
-
A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
-
Determination_of_cell_specific_regulatory_enhancers_in_hematopoetic_models
Study
EGAS00001000586
-
Measuring the level of relatedness between NGS datasets
Study
EGAS00001000600
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Study
EGAS00001000625
-
Genome of the Netherlands
Study
EGAS00001000644
-
A Genomics-Based Classification of Human Lung Tumors
Study
EGAS00001000647
-
Microsatellite data show recent demographic expansions in sedentary but not in nomadic human populations in Africa and Eurasia.
Study
EGAS00001000652
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
-
Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing
Study
EGAS00001000667
-
Study on the consequences of prenatal famine exposure on DNA methylation.
Study
EGAS00001000668
-
Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Study
EGAS00001000734
-
Next generation sequencing of sporadic schwannomatosis samples
Study
EGAS00001000767
-
Systems biology of Colorectal Cancer
Study
EGAS00001000854
-
Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883